Lupus Foundation of Jamaica

Lupus Foundation of Jamaica Using knowledge & support to combat this disease...Spreading Lupus awareness in Jamaica Lupus butterflies are different from all other butterflies.

We have the ability to flap our wings against the wind and ascend to great heights even though our wings are often achy... or sometimes broken. Ƹ̵̡Ӝ̵̨̄Ʒ...♪♫.¸¸♥Butterfly fly away♥¸¸.♫♪...Ƹ̵Ӝ̵̨̄Ʒ

Truth is, lupus is far more common than many people realize, yet so many still know very little about it. Beyond the phy...
10/05/2026

Truth is, lupus is far more common than many people realize, yet so many still know very little about it. Beyond the physical pain, lupus affects individuals emotionally, mentally, and financially every single day. Behind many smiles are silent battles the world may never fully see or understand.

This is why awareness matters. By speaking up, educating others, and showing support, we help make lupus visible and remind every warrior that they are not alone in their fight. 💜

09/05/2026

💜 Day 9: 10 Voices of Lupus 💜

As we reach the penultimate day of our countdown to World Lupus Day, we are leaning into the spiritual and mental strength required to navigate this journey.

✨ Meet Novianna Allen

Novianna doesn’t sugarcoat the reality of an SLE diagnosis. She vividly remembers the terrifying questions that flooded her mind at the start: "Am I going to die? Can it be treated? Is there a cure?" She acknowledges that Lupus is a total - body battle - it impacts you physically, financially, and mentally. But through those challenges, Novianna has found a profound sense of faith. She reminds us all that while the road isn't easy, it also isn’t always filled with bad days.

Her 3-step guide for those newly diagnosed:
1️⃣ Pray – Lean on your faith for strength.
2️⃣ Medicate – Be diligent with your treatment.
3️⃣ Think Positively – Guard your mindset fiercely.

Novianna is living proof that while Lupus changes your life, it cannot diminish your spirit. 🌟

Believe it or not, lupus disproportionately affects women. With 9 out of 10 persons living with the disease being female...
09/05/2026

Believe it or not, lupus disproportionately affects women. With 9 out of 10 persons living with the disease being female. 💜

Behind the makeup, the smiles, the careers, the motherhood, and the everyday routines… many women are silently fighting pain, fatigue, inflammation, and uncertainty every single day.

Lupus may be invisible to the eye, but its impact is very real.

Happy Saturday 💜Every day may not be easy, but every day, lupus warriors choose strength, courage, and hope. Behind the ...
09/05/2026

Happy Saturday 💜
Every day may not be easy, but every day, lupus warriors choose strength, courage, and hope. Behind the smiles are battles many people never see…the fatigue, the pain, the flare-ups, and the “but you don’t look sick” comments.

Today is a reminder that you are more than your diagnosis. You are powerful. You are resilient. You are STILL shining. 💪🏾✨

Let’s continue to make lupus visible, spread awareness, and stand together for every warrior fighting silently every day. 💜

Drop a 💜 in the comments to show your support for lupus warriors everywhere.

A heartfelt thank you to GraceKennedy Limited and Food For The Poor Jamaica for the lovely care packages that helped us ...
09/05/2026

A heartfelt thank you to GraceKennedy Limited and Food For The Poor Jamaica for the lovely care packages that helped us bring smiles, comfort, and support to our Lupus warriors ahead of International Lupus Day 2026 💜✨

Your generosity and partnership continue to make a meaningful impact, reminding our warriors that they are seen, supported, and never alone in this journey.

A special thank you to DLE Eatery for this beautiful cake and for showing love and support to our Lupus warriors ahead o...
09/05/2026

A special thank you to DLE Eatery for this beautiful cake and for showing love and support to our Lupus warriors ahead of International Lupus Day 2026 💜🎂

Your kindness and support helped make our Lupus Games Night even more special. We truly appreciate you for standing with our warriors and helping to spread awareness, encouragement, and hope within the community. ✨

💜

Earlier tonight, ahead of International Lupus Day 2026, warriors, supporters, families, and friends came together for an...
09/05/2026

Earlier tonight, ahead of International Lupus Day 2026, warriors, supporters, families, and friends came together for an unforgettable Lupus Games Night filled with laughter, fellowship, strength, and unity 💜✨

More than just games, it was a reminder that no warrior fights alone. Every smile shared, every conversation had, and every moment celebrated reflected the power of community, awareness, and support as we continue standing together in the fight against Lupus.

One night. One community. One powerful cause. 💜🎲
Check out these highlights ✨


08/05/2026

💜 Day 8: 10 Voices of Lupus 💜

Fear often stems from the unknown, but community has the power to turn that fear into strength. Today, we share a deeply personal chapter of the Lupus journey.

✨ Meet Verna Cassells

When Verna first received her diagnosis, her heart sank. Having recently lost a relative to Lupus, the news felt heavy and frightening. However, she wasn’t left to face it alone - a fellow Lupus Warrior stepped in, offering the guidance and hope Verna needed to realize that her story could have a different outcome.

Verna’s daily battle involves navigating the environment around her. She speaks candidly about:

☀️ The Sun: How the heat and UV rays can trigger intense challenges, making certain days a true test of endurance.

🥗 Fuel as Medicine: Verna considers her diet the "master key" to her health. By avoiding fatty foods and relying on a vibrant intake of fruits and vegetables, she sustains her energy and manages her symptoms.

🤝 The Power of Talk: For Verna, coping isn't just about medicine; it’s about connection. Having someone to talk to who truly understands the "Lupus life" is her ultimate support system.

Thank you, Verna, for showing us that while the triggers are real, so is the power of a warrior's resolve!

OneVoice OneCommunity OneFight

07/05/2026

As World Lupus Day 💜rapidly approaches, the conversation around lupus is becoming more urgent than ever. This morning, Dr. Desiree Tulloch-Reid and lupus warrior Danielle Hall joined host Dahlia Harris on Smile Jamaica to shine a spotlight on the realities of living with lupus and the importance of making this invisible illness visible.

From chronic pain and fatigue to the emotional and financial toll, the discussion highlighted why greater awareness, understanding, and support are needed now more than ever. Lupus affects thousands across Jamaica and the world, yet many still suffer in silence because their illness cannot always be seen.

💜 We are encouraging every Jamaican to wear PURPLE this Friday straight through to May 10 as we observe International World Lupus Day under the global theme “Make Lupus Visible” and the local call: “One Voice. One Community. One Fight.”

Whether you are a survivor, caregiver, friend, family member, school, business, church, or organization — your purple can spark a conversation, show solidarity, and help someone living with lupus feel seen.

Let’s light up Jamaica in purple.
Let’s raise awareness.
Let’s stand together for every lupus warrior fighting battles the world cannot always see.

07/05/2026

💜 Day 7: 10 Voices of Lupus 💜

The road to a Lupus diagnosis is rarely a straight line. It is often a journey through uncertainty, but finding the answer is the first step toward reclaiming your life.

✨ Meet Danielle Hall

Danielle speaks openly about the grueling process of misdiagnosis and the relief - and weight - of finally receiving a clear answer. That diagnosis was the key to unlocking the proper treatment she needed, yet the battle didn't end there.

For Danielle, the reality of Lupus involves navigating daily chronic pain. It is a constant companion that requires immense physical and mental fortitude. Because the burden can be so heavy, she emphasizes one vital truth: No one should fight this alone.

Support looks different for everyone - sometimes it’s a ride to a doctor’s visit, a meal during a flare, or simply a friend who listens without judgment. Danielle reminds us that "One Community" isn't just a hashtag; it’s a lifeline.

Let’s be that community for each other. 💜

OneVoice OneCommunity OneFight

Lupus may be invisible to many, but for thousands of warriors and families, the fight is real every single day. 💜This Wo...
07/05/2026

Lupus may be invisible to many, but for thousands of warriors and families, the fight is real every single day. 💜

This World Lupus Day, (May 10, 2026) let’s raise awareness, spark conversations, and stand together in support of those living with lupus. Wear purple. Share the message. Use your voice.

MAKE LUPUS VISIBLE. ✨

LupusWarrior JamaicaSupportsLupus

Address

National Volunteer Center, Suite5, 2D Camp Road, Kingston 4
Kingston
KINGSTON10

Opening Hours

Monday 09:00 - 16:00
Tuesday 09:00 - 16:00
Wednesday 09:00 - 16:00
Thursday 09:00 - 16:00
Friday 09:00 - 16:00

Telephone

+18767548458

Alerts

Be the first to know and let us send you an email when Lupus Foundation of Jamaica posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Lupus Foundation of Jamaica:

Share